HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921480Generated: October 30, 2026
Trimethylolpropane → HCID 86708418, compound
https://huagongshe.com/reaction/921480
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylolpropane | HCID 6510 | — |
| Reactant | 1-Bromononane | HCID 12742 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Product | HCID 86708418 | HCID 86708418 | — |
Reaction Steps
Under nitrogen stream, to a 2-L reactor provided with a stirrer, thermometer, condenser and gas inlet tube, 107.3 g (0.8 mol) of trimethylolpropane and 249 g (1.2 mol) of n-nonyl bromide and 11.4 g of tetrabutyl ammonium bromide were put, to which 360 g of 50 mass/volume % aqueous sodium hydroxide was added and heated at 70 to 80 degrees C. for four hours with stirring. After the reaction, the mixture was cooled and left still overnight to deposit white crystal. A liquid layer is transferred to a separating funnel by decantation. An alkali layer of an under layer was removed by separation. An organic layer was washed with 400 mL of saturated saline and 50 mL of a dilute aqueous solution of sulfuric acid. After the organic layer was further washed with distilled water until becoming neutral, 190 g of the obtained organic layer was dried with magnesium sulfate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273264B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-80a42cb71b1a418fb8dde8eaded63734 |
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| Source note | uspto-grants-2016_03 |
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